Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion type Assertion NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_head.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion wasGeneratedBy ECO_0000203 NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion wasDerivedFrom lhgdn-20090331 NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion SIO_000772 15235026 NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion evidence source_evidence_literature NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion description "[A patient with typical clinical and neuroradiological features of Leigh syndrome and cytochrome oxidase deficiency was found to have a mutation in the COX15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.